-
4
-
-
37049108419
-
-
For examples, see: a
-
For examples, see: (a) Grigg, R.; Thianpatanagul, S. J. Chem. Soc., Chem. Commun. 1984, 180.
-
(1984)
J. Chem. Soc., Chem. Commun
, pp. 180
-
-
Grigg, R.1
Thianpatanagul, S.2
-
5
-
-
37049099986
-
-
(b) Grigg, R.; Aly, M. F.; Sridharan, V.; Thianpatanagul, S. J. Chem. Soc., Chem. Commun. 1984, 182.
-
(1984)
J. Chem. Soc., Chem. Commun
, pp. 182
-
-
Grigg, R.1
Aly, M.F.2
Sridharan, V.3
Thianpatanagul, S.4
-
6
-
-
37049090900
-
-
(c) Ardill, H.; Grigg, R.; Sridharan, V.; Surendrakumar, S.; Thianpatanagul, S.; Kanajun, S. J. Chem. Soc., Chem. Commun. 1986, 602.
-
(1986)
J. Chem. Soc., Chem. Commun
, pp. 602
-
-
Ardill, H.1
Grigg, R.2
Sridharan, V.3
Surendrakumar, S.4
Thianpatanagul, S.5
Kanajun, S.6
-
7
-
-
12644310865
-
-
(d) Grigg, R.; Idle, J.; McMeekin, P.; Vipond, D. J. Chem. Soc., Chem. Commun. 1987, 49.
-
(1987)
J. Chem. Soc., Chem. Commun
, pp. 49
-
-
Grigg, R.1
Idle, J.2
McMeekin, P.3
Vipond, D.4
-
8
-
-
48049099665
-
-
(e) Grigg, R.; Kilner, C.; Sarker, M. A. B.; Orgaz de la Cierva, C.; Dondas, H. A. Tetrahedron 2008, 64, 8974.
-
(2008)
Tetrahedron
, vol.64
, pp. 8974
-
-
Grigg, R.1
Kilner, C.2
Sarker, M.A.B.3
Orgaz de la Cierva, C.4
Dondas, H.A.5
-
9
-
-
0039338892
-
-
For selected reviews, see: (a) Padwa, A, Ed, Wiley: New York, NY
-
For selected reviews, see: (a) Padwa, A., Ed. 1,3-Dipolar Cycloaddition Chemistry, Vol. 1; Wiley: New York, NY, 1984; p 817.
-
(1984)
1,3-Dipolar Cycloaddition Chemistry
, vol.1
, pp. 817
-
-
-
10
-
-
84910004125
-
-
Padwa, A, Ed, Wiley: New York, NY
-
(b) Padwa, A., Ed. 1,3-Dipolar Cycloaddition Chemistry, Vol. 2.; Wiley: New York, NY, 1984; p 704.
-
(1984)
1,3-Dipolar Cycloaddition Chemistry
, vol.2
, pp. 704
-
-
-
11
-
-
77249162730
-
-
Wiley: Chichester, U.K
-
(c) Padwa, A.; Pearson, W. H. Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products; Wiley: Chichester, U.K., 2002; Vol. 59, p 940.
-
(2002)
Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products
, vol.59
, pp. 940
-
-
Padwa, A.1
Pearson, W.H.2
-
14
-
-
33751433159
-
-
(f) Pandey, G.; Banerjee, P.; Gadre, S. R. Chem. Rev. 2006, 106, 4484.
-
(2006)
Chem. Rev
, vol.106
, pp. 4484
-
-
Pandey, G.1
Banerjee, P.2
Gadre, S.R.3
-
15
-
-
0002845373
-
-
Azomethine ylides are known to engage in 1,5- or 1,7-electrocyclizations: (a) Arany, A.; Bendell, D.; Groundwater, P. W.; Garnett, I.; Nyerges, M. J. Chem. Soc., Perkin Trans. 1999, 1, 2605.
-
Azomethine ylides are known to engage in 1,5- or 1,7-electrocyclizations: (a) Arany, A.; Bendell, D.; Groundwater, P. W.; Garnett, I.; Nyerges, M. J. Chem. Soc., Perkin Trans. 1999, 1, 2605.
-
-
-
-
16
-
-
22544481128
-
-
(b) Nyerges, M.; Pinter, A.; Viranyi, A.; Blasko, G.; Toke, L. Tetrahedron 2005, 61, 8199.
-
(2005)
Tetrahedron
, vol.61
, pp. 8199
-
-
Nyerges, M.1
Pinter, A.2
Viranyi, A.3
Blasko, G.4
Toke, L.5
-
18
-
-
0039046416
-
-
Cohen, N.; Blount, J. F.; Lopresti, R. J.; Trullinger, D. P. J. Org. Chem. 1979, 44, 4005.
-
(1979)
J. Org. Chem
, vol.44
, pp. 4005
-
-
Cohen, N.1
Blount, J.F.2
Lopresti, R.J.3
Trullinger, D.P.4
-
19
-
-
40149096724
-
-
(a) Zhang, C.; De, C. K.; Mal, R.; Seidel, D. J. Am. Chem. Soc. 2008, 130, 416.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 416
-
-
Zhang, C.1
De, C.K.2
Mal, R.3
Seidel, D.4
-
20
-
-
59649112358
-
-
(b) Murarka, S.; Zhang, C.; Konieczynska, M. D.; Seidel, D. Org. Lett. 2009, 11, 129.
-
(2009)
Org. Lett
, vol.11
, pp. 129
-
-
Murarka, S.1
Zhang, C.2
Konieczynska, M.D.3
Seidel, D.4
-
21
-
-
58149293587
-
-
(c) Zhang, C.; Murarka, S.; Seidel, D. J. Org. Chem. 2009, 74, 419.
-
(2009)
J. Org. Chem
, vol.74
, pp. 419
-
-
Zhang, C.1
Murarka, S.2
Seidel, D.3
-
22
-
-
70349399209
-
-
(d) Murarka, S.; Deb, I.; Zhang, C.; Seidel, D. J. Am. Chem. Soc. 2009, 131, 13226.
-
(2009)
J. Am. Chem. Soc
, vol.131
, pp. 13226
-
-
Murarka, S.1
Deb, I.2
Zhang, C.3
Seidel, D.4
-
23
-
-
43549110570
-
-
Zheng, L.; Yang, F.; Dang, Q.; Bai, X. Org. Lett. 2008, 10, 889.
-
(2008)
Org. Lett
, vol.10
, pp. 889
-
-
Zheng, L.1
Yang, F.2
Dang, Q.3
Bai, X.4
-
24
-
-
58249108032
-
-
(a) Bi, H.-P.; Zhao, L.; Liang, Y.-M.; Li, C.-J. Angew. Chem., Int. Ed. 2009, 48, 792.
-
(2009)
Angew. Chem., Int. Ed
, vol.48
, pp. 792
-
-
Bi, H.-P.1
Zhao, L.2
Liang, Y.-M.3
Li, C.-J.4
-
25
-
-
68149126726
-
-
(b) Bi, H.-P.; Chen, W.-W.; Liang, Y.-M.; Li, C.-J. Org. Lett. 2009, 11, 3246.
-
(2009)
Org. Lett
, vol.11
, pp. 3246
-
-
Bi, H.-P.1
Chen, W.-W.2
Liang, Y.-M.3
Li, C.-J.4
-
26
-
-
0037174448
-
-
Metal catalyzed decarboxylative couplings have recently emerged as valuable synthetic tools. For examples, see: a
-
Metal catalyzed decarboxylative couplings have recently emerged as valuable synthetic tools. For examples, see: (a) Myers, A. G.; Tanaka, D.; Mannion, M. R. J. Am. Chem. Soc. 2002, 124, 11250.
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 11250
-
-
Myers, A.G.1
Tanaka, D.2
Mannion, M.R.3
-
28
-
-
33746929476
-
-
(c) Goossen, L. J.; Deng, G.; Levy, L. M. Science 2006, 313, 662.
-
(2006)
Science
, vol.313
, pp. 662
-
-
Goossen, L.J.1
Deng, G.2
Levy, L.M.3
-
29
-
-
56849106003
-
-
For selected examples of recent contributions by others, see: a
-
For selected examples of recent contributions by others, see: (a) Polonka-Balint, A.; Saraceno, C.; Ludányi, K.; Bényei, A.; Matyus, P. Synlett 2008, 2846.
-
(2008)
Synlett
, pp. 2846
-
-
Polonka-Balint, A.1
Saraceno, C.2
Ludányi, K.3
Bényei, A.4
Matyus, P.5
-
31
-
-
54749085339
-
-
(c) Yeom, H.-S.; Lee, J.-E.; Shin, S. Angew. Chem., Int. Ed. 2008, 47, 7040.
-
(2008)
Angew. Chem., Int. Ed
, vol.47
, pp. 7040
-
-
Yeom, H.-S.1
Lee, J.-E.2
Shin, S.3
-
34
-
-
67749147313
-
-
(f) Ruble, J. C.; Hurd, A. R.; Johnson, T. A.; Sherry, D. A.; Barbachyn, M. R.; Toogood, P. L.; Bundy, G. L.; Graber, D. R.; Kamilar, G. M. J. Am. Chem. Soc. 2009, 131, 3991.
-
(2009)
J. Am. Chem. Soc
, vol.131
, pp. 3991
-
-
Ruble, J.C.1
Hurd, A.R.2
Johnson, T.A.3
Sherry, D.A.4
Barbachyn, M.R.5
Toogood, P.L.6
Bundy, G.L.7
Graber, D.R.8
Kamilar, G.M.9
-
35
-
-
67749142078
-
-
(g) Shikanai, D.; Murase, H.; Hata, T.; Urabe, H. J. Am. Chem. Soc. 2009, 131, 3166.
-
(2009)
J. Am. Chem. Soc
, vol.131
, pp. 3166
-
-
Shikanai, D.1
Murase, H.2
Hata, T.3
Urabe, H.4
-
36
-
-
68049099258
-
-
(h) Tobisu, M.; Nakai, H.; Chatani, N. J. Org. Chem. 2009, 74, 5471.
-
(2009)
J. Org. Chem
, vol.74
, pp. 5471
-
-
Tobisu, M.1
Nakai, H.2
Chatani, N.3
-
37
-
-
67650682825
-
-
(i) Frank, E.; Schneider, G.; Kadar, Z.; Woelfling, J. Eur. J. Org. Chem. 2009, 3544.
-
(2009)
Eur. J. Org. Chem
, pp. 3544
-
-
Frank, E.1
Schneider, G.2
Kadar, Z.3
Woelfling, J.4
-
38
-
-
67649342031
-
-
(j) Mahoney, S. J.; Moon, D. T.; Hollinger, J.; Fillion, E. Tetrahedron Lett. 2009, 50, 4706.
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 4706
-
-
Mahoney, S.J.1
Moon, D.T.2
Hollinger, J.3
Fillion, E.4
-
39
-
-
67650473037
-
-
(k) Mori, K.; Ohshima, Y.; Ehara, K.; Akiyama, T. Chem. Lett. 2009, 38, 524.
-
(2009)
Chem. Lett
, vol.38
, pp. 524
-
-
Mori, K.1
Ohshima, Y.2
Ehara, K.3
Akiyama, T.4
-
40
-
-
70149095459
-
-
(l) Han, S. B.; Kim, I. S.; Han, H.; Krische, M. J. J. Am. Chem. Soc. 2009, 131, 6916.
-
(2009)
J. Am. Chem. Soc
, vol.131
, pp. 6916
-
-
Han, S.B.1
Kim, I.S.2
Han, H.3
Krische, M.J.4
-
41
-
-
70349769724
-
-
(a) Burns, N. Z.; Baran, P. S.; Hoffmann, R. W. Angew. Chem., Int. Ed. 2009, 48, 2854.
-
(2009)
Angew. Chem., Int. Ed
, vol.48
, pp. 2854
-
-
Burns, N.Z.1
Baran, P.S.2
Hoffmann, R.W.3
-
42
-
-
70350500463
-
-
(b) Newhouse, T.; Baran, P. S.; Hoffmann, R. W. Chem. Soc. Rev. 2009, 38, 3010.
-
(2009)
Chem. Soc. Rev
, vol.38
, pp. 3010
-
-
Newhouse, T.1
Baran, P.S.2
Hoffmann, R.W.3
-
43
-
-
34250769398
-
-
For an excellent review on the R-functionalization of amines, see
-
For an excellent review on the R-functionalization of amines, see: Campos, K. R. Chem. Soc. Rev. 2007, 36, 1069.
-
(2007)
Chem. Soc. Rev
, vol.36
, pp. 1069
-
-
Campos, K.R.1
-
44
-
-
0000804243
-
-
Orsini, F.; Pelizzoni, F.; Forte, M.; Destro, R.; Gariboldi, P. Tetrahedron 1988, 44, 519.
-
(1988)
Tetrahedron
, vol.44
, pp. 519
-
-
Orsini, F.1
Pelizzoni, F.2
Forte, M.3
Destro, R.4
Gariboldi, P.5
-
45
-
-
33751555599
-
-
Lakhdar, S.; Westermaier, M.; Terrier, F.; Goumont, R.; Boubaker, T.; Ofial, A. R.; Mayr, H. J. Org. Chem. 2006, 71, 9088.
-
(2006)
J. Org. Chem
, vol.71
, pp. 9088
-
-
Lakhdar, S.1
Westermaier, M.2
Terrier, F.3
Goumont, R.4
Boubaker, T.5
Ofial, A.R.6
Mayr, H.7
-
46
-
-
75749123474
-
-
After the submission of this manuscript, the formation of products 8 under similar conditions was reported: Bi, H.-P.; Teng, Q.; Guan, M.; Chen, W.-W.; Liang, Y.-M.; Yao, X.; Li, C.-J. J. Org. Chem. 2010 (DOI: 10.1021/ jo902319h).
-
After the submission of this manuscript, the formation of products 8 under similar conditions was reported: Bi, H.-P.; Teng, Q.; Guan, M.; Chen, W.-W.; Liang, Y.-M.; Yao, X.; Li, C.-J. J. Org. Chem. 2010 (DOI: 10.1021/ jo902319h).
-
-
-
-
47
-
-
77249156368
-
-
The use of lower amounts of benzoic acid gave rise to lower yields
-
The use of lower amounts of benzoic acid gave rise to lower yields.
-
-
-
|